Renaforce - 57520-0303-1 - (Berberis vulgaris, Echinacea angustifolia, Coccus cacti, Kali muriaticum, Lycopodium clavatum, Nitricum acidum,)

Alphabetical Index


Drug Information of Renaforce

Product NDC: 57520-0303
Proprietary Name: Renaforce
Non Proprietary Name: Berberis vulgaris, Echinacea angustifolia, Coccus cacti, Kali muriaticum, Lycopodium clavatum, Nitricum acidum,
Active Ingredient(s): 3; 3; 12; 12; 12; 12    [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL & nbsp;   Berberis vulgaris, Echinacea angustifolia, Coccus cacti, Kali muriaticum, Lycopodium clavatum, Nitricum acidum,
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Renaforce

Product NDC: 57520-0303
Labeler Name: Apotheca Company
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20101102

Package Information of Renaforce

Package NDC: 57520-0303-1
Package Description: 30 mL in 1 BOTTLE, DROPPER (57520-0303-1)

NDC Information of Renaforce

NDC Code 57520-0303-1
Proprietary Name Renaforce
Package Description 30 mL in 1 BOTTLE, DROPPER (57520-0303-1)
Product NDC 57520-0303
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Berberis vulgaris, Echinacea angustifolia, Coccus cacti, Kali muriaticum, Lycopodium clavatum, Nitricum acidum,
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20101102
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Apotheca Company
Substance Name BERBERIS VULGARIS ROOT BARK; ECHINACEA ANGUSTIFOLIA; LYCOPODIUM CLAVATUM SPORE; NITRIC ACID; POTASSIUM CHLORIDE; PROTORTONIA CACTI
Strength Number 3; 3; 12; 12; 12; 12
Strength Unit [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
Pharmaceutical Classes

Complete Information of Renaforce


General Information